-
Job Description
Join a leading multinational medical device organization in Limerick as a key player in product quality and process improvement.
We're seeking a highly skilled professional to drive continuous improvement and optimize product quality and process yield.
Key Responsibilities:
- Develop and execute plans to improve product quality and process yield through process characterization and optimization.
- Identify and implement process-related continuous improvement activities to enhance product quality and Overall Equipment Effectiveness.
- Ensure all process developments and improvements meet Quality Management System requirements (ISO 13485, FDA & JPAL).
- Lead the team with a clear work ethos and engage with personnel to resolve Corrective/Preventative actions.
- Manage projects with accurate planning, timely delivery, and reporting.
- Participate in risk assessments and HAZOPs of manufacturing processes and equipment.
- Develop and maintain Behavioural Standards in line with company standards and policy.
- Stay up-to-date on new developments and technologies in assigned disciplines and present on new Best Practice methodologies.
Requirements:
- Primary Degree (Level 8) in Process, Production, Manufacturing, Polymer, Materials, Biomedical or Mechanical engineering.
- Minimum 4 years' experience in a regulated environment.
- Relevant experience with statistical process control and capability analysis.
- Excellent analytical and problem-solving skills, root cause analysis, and risk assessments.